chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56316429	56316430	G	C	63	GENIC	homozygous	109738376
19	56319857	56319858	G	A	41	GENIC	homozygous	109738380
19	56320468	56320469	A	G	36	GENIC	homozygous	109738382
19	56323710	56323711	C	T	36	GENIC	homozygous	109738384
19	56323790	56323791	C	T	37	GENIC	homozygous	109738386
19	56324840	56324841	T	C	37	GENIC	homozygous	109738388
19	56327463	56327464	T	C	38	GENIC	homozygous	109738390
19	56329037	56329038	A	G	34	GENIC	homozygous	109738392
19	56317349	56317349		A	30	GENIC	homozygous	129623386
19	56328067	56328067		A	15	GENIC	homozygous	129623387
19	56329567	56329568	T	C	35	GENIC	homozygous	119633753
19	56329673	56329678	CCTGC		47	GENIC	homozygous	129623388
19	56330031	56330032	G	A	44	GENIC	homozygous	109738394
19	56331015	56331015		CTG	54	GENIC	homozygous	129623389
19	56331018	56331021	CCC		54	GENIC	homozygous	129623390
19	56331021	56331022	C	A	54	GENIC	homozygous	109738396
19	56331038	56331038		TC	42	GENIC	homozygous	129623391
19	56331700	56331701	A	T	41	GENIC	homozygous	109738398
19	56331834	56331835	A	G	37	GENIC	homozygous	109738400
19	56331903	56331904	G	A	42	GENIC	homozygous	109738402
19	56332006	56332007	A	G	43	GENIC	homozygous	109738404
19	56332572	56332573	G	A	45	GENIC	homozygous	109738406
19	56332602	56332603	G	T	37	GENIC	homozygous	109738408
19	56333272	56333273	C	T	41	GENIC	possibly homozygous	109738410
19	56333651	56333652	A	T	43	GENIC	homozygous	109738412
19	56333857	56333858	C	T	41	GENIC	homozygous	109738414
19	56334558	56334559	A	G	38	GENIC	homozygous	109738416
19	56335185	56335196	CAGAGGAAGTC		6	GENIC	homozygous	129623392
19	56335440	56335441	C	T	34	GENIC	homozygous	109738418
19	56335441	56335442	G	A	32	GENIC	homozygous	109738420
19	56335443	56335444	A	C	33	GENIC	homozygous	109738422